Low-affinity ligands for the TCR drive proliferation of mature CD8+ T cells in lymphopenic hosts.
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Aging, autoimmunity and arthritis: T-cell senescence and contraction of T-cell repertoire diversity - catalysts of autoimmunity and chronic inflammationTargeting Homeostatic T Cell Proliferation to Control Beta-Cell AutoimmunityT cell metabolism drives immunityIndoctrinating T cells to attack pathogens through homeschoolingRheumatoid arthritis: a role for immunosenescence?CD24 expression on T cells is required for optimal T cell proliferation in lymphopenic hostMassive and destructive T cell response to homeostatic cue in CD24-deficient lymphopenic hostsEstimating the diversity, completeness, and cross-reactivity of the T cell repertoire.The dynamics of T-cell receptor repertoire diversity following thymus transplantation for DiGeorge anomalyModulating T-cell homeostasis with IL-7: preclinical and clinical studies.Heat shock protein vaccination and directed IL-2 therapy amplify tumor immunity rapidly following bone marrow transplantation in mice.Niche recycling through division-independent egress of hematopoietic stem cellsAn overview of IL-7 biology and its use in immunotherapy.IL-2 mediates CD4+ T cell help in the breakdown of memory-like CD8+ T cell tolerance under lymphopenic conditionsHomeostatic proliferation is a barrier to transplantation tolerance.Adjuvant IL-7 or IL-15 overcomes immunodominance and improves survival of the CD8+ memory cell pool.Cell-to-cell interactions and signals involved in the reconstitution of peripheral CD8 T(CM) and T(EM) cell pools.Simultaneous detection of circulating autoreactive CD8+ T-cells specific for different islet cell-associated epitopes using combinatorial MHC multimers.Homeostatic T cell proliferation: how far can T cells be activated to self-ligands?Homeostatic T cell proliferation in a T cell-dendritic cell coculture system.Different contributions of thymopoiesis and homeostasis-driven proliferation to the reconstitution of naive and memory T cell compartmentsNaive T cells proliferate strongly in neonatal mice in response to self-peptide/self-MHC complexes.Dependence of lymphopenia-induced T cell proliferation on the abundance of peptide/ MHC epitopes and strength of their interaction with T cell receptors.Redirecting the immune response: role of adoptive T cell therapy.Role for Bcl-6 in the generation and maintenance of memory CD8+ T cells.Tissue specific deletion of inhibitor of kappa B kinase 2 with OX40-Cre reveals the unanticipated expression from the OX40 locus in skin epidermis.Lymphodepletion is permissive to the development of spontaneous T-cell responses to the self-antigen PR1 early after allogeneic stem cell transplantation and in patients with acute myeloid leukemia undergoing WT1 peptide vaccination following chemotHomeostasis of alpha beta TCR+ T cells.Peripheral T-cell tolerance defined through transgenic mouse studies.The immunology of Epstein-Barr virus infectionCross-reactivity in T-cell antigen recognition.IL-7 in human health and disease.How the immune system works to protect the host from infection: a personal view.The importance of LAT in the activation, homeostasis, and regulatory function of T cellsIL-18 synergizes with IL-7 to drive slow proliferation of naive CD8 T cells by costimulating self-peptide-mediated TCR signals.T cell homeostasis and systemic autoimmunityA peripheral CD4+ T cell precursor for naive, memory, and regulatory T cellsSelf-specific CD8+ T cells maintain a semi-naive state following lymphopenia-induced proliferation.Cytokine requirements for acute and Basal homeostatic proliferation of naive and memory CD8+ T cells.Fas (CD95/APO-1) limits the expansion of T lymphocytes in an environment of limited T-cell antigen receptor/MHC contacts
P2860
Q24797866-CD25B231-9775-49C0-B124-81950A6559FCQ26764999-6510B517-64BD-4A3D-BA47-923E911A890BQ26799575-36EB9B4E-34A1-48F8-9E40-2A04BDFEC8F3Q27012849-BD1AE6C9-85E9-4720-B9DB-6CDED89DC2F2Q27693905-9F61D8C6-B0A4-4B30-A5F1-A7B2BE2687C5Q28589464-EC414871-6360-4B8D-930E-45A2B9E654C9Q28592601-94D00D82-E5A3-4913-84AC-FD05CED079D1Q33357547-16F44D7E-333D-490C-A711-99DF16E03BB8Q33466761-1E1F04E7-451E-45B5-904B-C3FD656C22C6Q33553984-ED9FE4C2-EAD5-4DB6-83F6-615A2F62AF88Q33585305-68FD3E8D-BCA2-4CEF-A5EB-931117DB5B41Q33591065-71E4C5EB-2203-44DA-840D-2E4FCD6F4066Q33678845-A75C1AA4-658C-4EAF-980E-D0948AE01A93Q33697777-F75B012A-9214-402B-B1AB-E8FED7BBA23BQ33731951-8F35A181-7FB4-4F2B-B0CE-8E6B02ADB3E0Q33736534-9A0097FF-0586-43C3-B689-2870A2204E2BQ33851766-36187E5A-14EC-4763-A84C-D1352DAF5EBCQ33930268-D88232AC-190F-4CD4-8F6E-79B1ED389736Q34010799-FE4BFB9F-FC79-4FD3-BA12-B5E13FA790D6Q34015676-B5C0C660-F335-48CD-8D83-EB2C182BFF31Q34015733-D03A082A-BA5F-476E-A733-AEACD559E7B7Q34048855-26585E6E-2E56-4A67-B1CF-6AB50230F9CCQ34100049-28BC1F9F-18FB-411D-B6C6-4430AFC45D21Q34123238-E279C8C3-9277-4D9B-B503-E92ECC857751Q34129480-7465CEBC-DDD7-4C74-AAAF-5FEDA45C0536Q34171710-ADC36810-9DC8-4BCD-B5A6-C11C4136681FQ34180369-3BCACEEF-9F72-4717-971E-EABBBBBE5235Q34180992-BAAFDB32-C0BD-44DB-95C0-037BCBB16E42Q34193042-9545F960-C64D-4586-A30A-77740DC78B6BQ34225567-42B1800C-3F15-444C-9B69-DB43206E8A35Q34249351-F2710375-B710-4A03-943F-1231C7FA67BAQ34260682-024E7C28-7344-49A6-AC7F-01CABAA24E74Q34272671-125AD29E-5BC7-4833-8460-90BD7729C1E7Q34285036-E33BCCB4-5AAB-4054-8F17-F5B9348A9FE6Q34289372-4C31ECB2-FAE9-40ED-93C5-BF05F51AAD9EQ34328737-C219E638-821D-4FF2-811B-3C2FC81E8FF4Q34420793-DB88FCF4-1FA4-465D-9B0F-EBFE81821A37Q34470833-7FAEF8E8-363C-4B85-8BF1-543D296B0EA6Q34524226-25221E5F-140A-433C-A289-C0D14A60DF23Q34538716-80F881E7-3EB5-4DB1-ABEC-8194BF8AEE00
P2860
Low-affinity ligands for the TCR drive proliferation of mature CD8+ T cells in lymphopenic hosts.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 1999
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@en
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@nl
type
label
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@en
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@nl
prefLabel
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@en
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@nl
P2860
P1433
P1476
Low-affinity ligands for the T ...... T cells in lymphopenic hosts.
@en
P2093
A W Goldrath
P2860
P304
P356
10.1016/S1074-7613(00)80093-X
P407
P577
1999-08-01T00:00:00Z